Myfortic and haemoglobin decreased Patient Reports February 12, 2012

Myfortic Side Effects Report #5443001-7
Myfortic side effect was reported by a Pharmacist from UNITED STATES on Aug 27, 2007. Female patient, 50 years of age, weighting 119.0 lb, was diagnosed with renal transplant and was treated with Myfortic. After drug was administered, patient experienced the following side effects: bacterial sepsis, blood creatinine increased, diarrhoea, haemoglobin decreased, hypotension, urinary tract infection , ventricular tachycardia. Myfortic dosage: 360 MG, BID. Patient was hospitalized. Patient recovered.

Myfortic Side Effects Report #5450845-4
Myfortic side effect was reported by a Pharmacist from UNITED STATES on Sept 04, 2007. Female patient, 50 years of age, weighting 119.0 lb, was diagnosed with renal transplant and was treated with Myfortic. After drug was administered, patient experienced the following side effects: bacterial sepsis, blood creatinine increased, diarrhoea, haemoglobin decreased, hypotension, urinary tract infection , ventricular tachycardia. Myfortic dosage: 360 MG, BID. Patient was hospitalized. Patient recovered.

Myfortic Side Effects Report #5461116-4
Myfortic side effect was reported by a Pharmacist from UNITED STATES on Sept 10, 2007. Female patient, 50 years of age, weighting 119.0 lb, was diagnosed with renal transplant and was treated with Myfortic. After drug was administered, patient experienced the following side effects: bacterial sepsis, blood creatinine increased, diarrhoea, haemoglobin decreased, hypotension, urinary tract infection , ventricular tachycardia. Myfortic dosage: 360 MG, BID. Patient was hospitalized. Patient recovered.

Myfortic Side Effects Report #5378124-4
Myfortic side effect was reported by a Physician from GERMANY on June 22, 2007. Male patient, 33 years of age, weighting 108.0 lb, was diagnosed with renal transplant and was treated with Myfortic. After drug was administered, patient experienced the following side effects: agranulocytosis, haemoglobin decreased, pyrexia, thrombocytopenia, white blood cell count decreased. Myfortic dosage: 576 MG/DAY. During the same period patient was treated with COTRIM DS, COTRIM DS, COTRIM DS, TORSEMIDE, AMPHO, KALINOR. Patient recovered.


Myfortic Side Effects Report #5389880-3
Myfortic side effect was reported by a Health Professional from GERMANY on July 12, 2007. Male patient, 33 years of age, weighting 108.0 lb, was diagnosed with renal transplant and was treated with Myfortic. After drug was administered, patient experienced the following side effects: agranulocytosis, haemoglobin decreased, pyrexia, thrombocytopenia, white blood cell count decreased. Myfortic dosage: 576 MG/DAY. During the same period patient was treated with COTRIM DS, COTRIM DS, COTRIM DS, TORSEMIDE, AMPHO, KALINOR. Patient recovered.

Myfortic Side Effects Report #5042537-0
Myfortic side effect was reported by a Physician from TURKEY on June 15, 2006. Female patient, 50 years of age, was diagnosed with pemphigus , candidiasis and was treated with Myfortic. After drug was administered, patient experienced the following side effects: blood calcium decreased, blood potassium decreased, blood sodium decreased, c-reactive protein increased, haematocrit decreased, haemoglobin decreased, red blood cell sedimentation rate increased. Myfortic dosage: unknown. During the same period patient was treated with FLUCONAZOLE. Patient was hospitalized. Patient died on 03/21/2006.

Myfortic Side Effects Report #6065217-1
Myfortic side effect was reported by a Physician from GERMANY on Jan 22, 2009. Male patient, 45 years of age, was diagnosed with corneal transplant and was treated with Myfortic. After drug was administered, patient experienced the following side effects: gastrointestinal disorder, glaucoma , haemoglobin decreased, intraocular pressure test abnormal, nausea , removal of transplanted organ. Myfortic dosage: 360 MG, BID. During the same period patient was treated with CORTICOSTEROID NOS. Patient recovered.

Myfortic Side Effects Report #6103732-2
Myfortic side effect was reported by a Physician from GERMANY on Feb 25, 2009. Male patient was diagnosed with corneal transplant, immunosuppression, glaucoma , intraocular pressure increased and was treated with Myfortic. After drug was administered, patient experienced the following side effects: gastrointestinal disorder, glaucoma , haemoglobin decreased, intraocular pressure increased, intraocular pressure test abnormal, nausea , removal of transplanted organ. Myfortic dosage: 360 MG, BID. During the same period patient was treated with CORTICOSTEROID NOS, GLAUPAX, DECORTIN. Patient recovered.